Regulatory affairs expert witnesses draw on careers in pharma, biotech, medical devices, and healthcare products to clarify compliance with FDA, EMA, and other regulatory frameworks. They evaluate submissions, labeling, quality systems, post-market surveillance, and risk management, and assess whether regulatory strategies, documentation, and decisions met applicable standards.
AED Program Design & Compliance Legal Expert Witness
AED Program Design & Compliance Legal Expert Witness
- Review Fee
- $300/hr
- Deposition Fee
- $500/hr
This highly-qualified expert has extensive experience in automated external defibrillator (AED) program design and compliance. He earned his BS in public affairs from the University of Oregon and his JD from the Lewis & Clark Northwestern School of Law. He is a member of the Oregon State Bar and an advisory board member of the Sudden Cardiac Arrest Foundation and the National Center for Early Defibrillation. He has been the founder of several firms, including Lazar Jensen Geobel, Fios, Inc., and AED Risk Insights, Inc. Currently, this expert is the founder and president of an AED program compliance company that develops and publishes national AED program design guidelines that describe industry standards for AED programs and the AED Law Center.
Founder and President, An AED program compliance company
Juris Doctor (JD), Lewis & Clark Northwestern School of Law
Oregon